ADHDgene Database
  • Published Variant
  • Published Gene: 359
  • Published Region: 128
  • Pathway by PBA: 8
  • Study: 361

SNP Report

Basic Info
Name rs1982406 dbSNP Ensembl
Location chr7:50597627(Fwd)
Variant Alleles A/G
Ancestral Allele A
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000357936; ENST00000380984; ENST00000426377; ENST00000430300; ENST00000431062; ENST00000444124; ENST00000444733; ENST00000489162)
nc_transcript_variant(ENST00000489162)
NMD_transcript_variant(ENST00000444733)
upstream_gene_variant(ENST00000454521)
No. of Studies 1 (significant: 1; non-significant: 0; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Ribases M, 2009(b) Case-control test: lowest P-value=0.022 for genotype analysi...... Case-control test: lowest P-value=0.022 for genotype analysis, P-value=0.1 for allele analysis in adult combined ADHD; lowest P-value=0.0044 for genotype analysis, P-value=0.0087 for allele analysis in all childhood ADHD; lowest P-value=0.00058 for genotype analysis, P-value=0.0031 for allele analysis in childhood combined ADHD. More... no significance after correcting for multiple comparisons no significance after correcting for multiple comparisons Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs1982406 (count: 18) View in gBrowse (chr7:50572709..50615840 )
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.

Literature-origin SNPs (count: 0)

LD-proxies (count: 18)